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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191766Generated: October 26, 2026

Toluene → Tert-butyl 2-(4-fluoroanilino)-4-(2-isopropoxyphenyl)benzoate

https://huagongshe.com/reaction/2191766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Isopropoxyphenylboronic acidHCID 5084099—
ReactantTert-butyl 4-bromo-2-(4-fluoroanilino)benzoateHCID 68956988—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(4-fluoroanilino)-4-(2-isopropoxyphenyl)benzoateHCID 68964024—

Reaction Steps

To toluene 1.6 mL solution of tert-butyl 4-bromo-2-(4-fluoroanilino)benzoate 70 mg were added ethanol 0.60 mL, water 0.30 mL, 2-isopropoxyphenylboronic acid 0.048 mL, sodium hydrogen carbonate 48 mg and tetrakis(triphenylphosphine)palladium(0) 11 mg at room temperature, and it was heated and refluxed for 6 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and water were added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, and the solvent was removed under reduced pressure. The obtained residue was refined by silica gel column chromatography [Trikonex company, Flash Tube 2008, eluent; hexane:ethyl acetate=5:1] to give tert-butyl 2-(4-fluoroanilino)-4-(2-isopropoxyphenyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-2646f07864eb4e208ee1e99a76fc424a
Source noteuspto-grants-2012_12